2 Fluoro 4 7 Quinolin 6 Ylmethyl Imidazo 1 2 B 1 2 4 Triazin 2 Yl Benzonitrile
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Fluoro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzonitrile
Chemical Formula C26H16FN5
Molecular Weight 421.44 g/mol
Appearance Solid (predicted)
Melting Point No data available
Boiling Point No data available
Solubility Insoluble in water (predicted), Soluble in organic solvents like DMSO (predicted)
Density No data available
Logp No data available
Pka No data available
Uv Vis Absorption Absorption peaks in UV - Vis region related to aromatic and heterocyclic chromophores (predicted)
Chemical Name 2-Fluoro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzonitrile
Chemical Name 2-Fluoro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzonitrile
Molecular Formula C24H15FN6
Molecular Weight 412.41 g/mol
Melting Point No experimental data available (predicted range might be based on similar structures)
Boiling Point No experimental data available (predicted to decompose before boiling based on structure complexity)
Solubility Poorly soluble in water (predicted due to non - polar aromatic nature), solubility in organic solvents like DMSO and DMF is expected to be better
Pka No experimental data available (predicted acidic groups' pKa would be relevant for its behavior in different pH environments)
Logp Positive value predicted (lipophilic due to aromatic rings, which affects its distribution in biological systems)
Density No experimental data available (estimated density based on similar aromatic compounds)
Chemical Formula C26H16FN5
Molecular Weight 421.44 g/mol
Solubility In Water Low (organic compound with non - polar regions)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (predicted based on structure)
Logp Predicted to be positive (lipophilic due to aromatic rings)
Pka No publicly available data (no obvious acidic or basic functional groups in the neutral form)
FAQ

What is the main use of 2-Fluoro-4- [7- (quinoline-6-ylmethyl) imidazo [1,2-b] [1,2,4] triazin-2-yl] benzonitrile

2-Fluoro-4- [7- (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile, which is an organic compound. Its main uses involve the field of pharmaceutical chemistry.

In the field of pharmaceutical research and development, such compounds are often key intermediates for the creation of new drugs. Due to their special molecular structure, or the ability to bind to specific targets in organisms, they exhibit unique biological activities. For example, they may inhibit or activate specific proteins or enzymes related to certain diseases for the purpose of treating diseases. In the research and development of anti-cancer drugs, researchers may hope to modify their structures to precisely act on the key signaling pathways of cancer cells, hinder the proliferation and migration of cancer cells, and induce their apoptosis, thus providing new strategies and ways to overcome cancer problems.

Furthermore, in the basic research of pharmaceutical chemistry, 2-fluoro-4- [7 - (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile can be used as a model compound to help researchers further explore the mechanism of drug-target interaction, structure-activity relationship and other basic scientific issues. By analyzing the patterns and characteristics of its combination with biological macromolecules, the rules can be summarized and the theoretical foundation for the design of more efficient and low-toxicity drugs can be laid.

In addition, in the field of organic synthetic chemistry, this compound can also be used as an important synthetic building block. Because its structure is rich in a variety of active functional groups, it can be spliced and modified with other compounds through a series of organic reactions to build more complex and specific functional organic molecules, expand the boundaries of organic synthesis, and provide material basis and technical support for the development of materials science, chemical biology and other related fields.

What are the chemical properties of 2-Fluoro-4- [7- (quinoline-6-ylmethyl) imidazo [1,2-b] [1,2,4] triazin-2-yl] benzonitrile

2-Fluoro-4- [7- (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile is an organic compound. Its chemical properties are unique, let me explain in detail.

First of all, its physical properties, the melting point and boiling point of this compound are often the focus of research. However, its specific values vary depending on the preparation and test conditions. Generally speaking, the melting point reflects the strength of intermolecular forces, and the boiling point is related to the energy required for gasification. In this compound structure, the structure of fluorine atoms, cyanyl groups and thick heterocycles affects the intermolecular interactions, resulting in a specific melting and boiling point range.

In addition to chemical stability, the structure of aromatic rings and heterocycles gives it a certain stability. The aromatic ring conjugated system can disperse electrons and reduce the reactivity. However, fluorine atoms have strong electronegativity, which reduces the electron cloud density of ortho-carbon atoms and easily initiates nucleophilic substitution reactions. Cyanyl groups are also active groups and can participate in many reactions such as hydrolysis and addition.

In terms of reactivity, the quinoline-6-yl methyl part, methyl hydrogen has a certain acidity, and can be taken away under the action of strong bases, triggering subsequent nucleophilic reactions. Imidazolo [1,2-b] [1,2,4] triazine ring, nitrogen atom is electron-rich, can be used as nucleophilic reagent to participate in the reaction, and can also coordinate with metal ions to form complexes.

In addition, this compound may have certain optical properties due to its polyaromatic ring structure. Under the irradiation of specific wavelengths of light, it may occur electron transition and exhibit fluorescence and other phenomena, which may have potential applications in the field of optical materials. Its chemical properties are complex and interesting, and it may have important uses in organic synthesis, pharmaceutical chemistry and other fields, which need to be further explored by researchers.

What is the synthesis method of 2-Fluoro-4- [7- (quinoline-6-ylmethyl) imidazo [1,2-b] [1,2,4] triazin-2-yl] benzonitrile

To obtain the synthesis method of 2-fluoro-4- [7 - (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile, the following method can be used.

First, various starting materials need to be prepared, such as fluorine-containing benzonitrile derivatives, related compounds with quinoline structures, and raw materials that can be used to construct imidazolo [1,2-b] [1,2,4] triazine structures. First, the fluorobenzonitrile derivatives are reacted with appropriate reagents to introduce specific substituents and lay the foundation for subsequent cyclization reactions. This reaction may need to be carried out under specific conditions of temperature, pressure and catalyst presence. For example, a certain type of metal catalyst can be selected to promote the smooth occurrence of the reaction and improve the reaction rate and yield.

Furthermore, the compound with the quinoline structure is treated to make its active check point easy to combine with other parts. This process may involve the conversion of functional groups. Through appropriate reaction conditions, the specific position of the quinoline compound is generated to produce an active group that can effectively react with the subsequent reactants.

Subsequently, the above-treated raw materials are mixed and a key cyclization reaction is carried out to form the imidazolo [1,2 - b] [1,2,4] triazine structure. This step requires precise control of the reaction conditions. If the temperature needs to be strictly maintained within a certain range, too high or too low may affect the efficiency of cyclization and the purity of the product. The pH of the reaction system also needs to be carefully adjusted, which can be achieved by adding suitable acid-base regulators. At the same time, the reaction time is also very important. According to the experimental monitoring results, it is necessary to ensure that the reaction is carried out to the right extent, neither excessive reaction leads to an increase in by-products, nor insufficient reaction and less product generation.

After the reaction is completed, it needs to go through the steps of separation and purification. The target product can be separated from the reaction mixture by means such as column chromatography and recrystallization, and impurities can be removed to obtain high-purity 2-fluoro-4- [7 - (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile. The whole synthesis process requires fine operation, and each step is closely linked to achieve the synthesis of the target product effectively.

2-Fluoro-4- [7- (quinoline-6-ylmethyl) imidazo [1,2-b] [1,2,4] triazin-2-yl] benzonitrile What are the safety precautions

2-Fluoro-4- [7- (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile is a chemical substance. Regarding its safety precautions, let me tell you in detail.

First of all, this chemical substance may be toxic. Because its structure contains many special groups, the contact routes are different and the hazards are different. If it comes into contact with the skin, it may cause skin irritation, such as erythema, itching, or even allergic reactions. Therefore, when operating, protective clothing and gloves must be worn to avoid skin contact. Upon contact, rinse with plenty of water as soon as possible. If you feel unwell, seek medical attention urgently.

If you inhale the substance dust or volatile gas, or damage the respiratory system, causing cough, asthma, breathing difficulties. Operate with good ventilation, and if conditions permit, use local exhaust equipment. If necessary, wear a gas mask to prevent inhalation hazards.

Furthermore, the risk of accidentally taking this chemical is extremely high, or it may cause serious symptoms such as burning of the digestive tract, abdominal pain, and vomiting. During operation, do not eat, smoke, keep the work area clean, and avoid contaminating food and water sources. If you accidentally take it by mistake, do not urge vomiting, seek medical attention quickly, and carry chemical information to help doctors diagnose and treat.

In addition, 2-fluoro-4- [7- (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile may be environmentally hazardous. When disposing and using, follow environmental regulations and do not dump it at will to prevent contamination of soil and water sources. Experimental waste is collected by classification and handed over to professional institutions for treatment.

Storage should not be ignored. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources, and stored separately from oxidants, acids and alkalis. Do not mix storage to prevent dangerous reactions.

In conclusion, when handling 2-fluoro-4- [7 - (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile, be cautious, be aware of safety precautions, and take appropriate protective measures to ensure personal safety and environmental safety.

What is the price range of 2-Fluoro-4- [7- (quinolin-6-ylmethyl) imidazo [1,2-b] [1,2,4] triazin-2-yl] benzonitrile in the market?

There is a question today, what is the price range of 2-fluoro-4- [7 - (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile in the market. However, it is difficult to determine the price of this product in the market. Its price often varies due to many reasons, and the abundance of raw materials, the difficulty of preparation, and the amount of demand all affect its price.

If the raw materials are abundant, the preparation method is simple, and the demand is not strong, the price may be slightly cheaper. On the contrary, if the raw materials are scarce, the preparation is complicated, and the demand is strong, the price will be high.

Looking at the prices of things in the past, they changed with time. Today's market conditions are changing rapidly. To determine the price of this 2-fluoro-4- [7- (quinoline-6-ylmethyl) imidazolo [1,2-b] [1,2,4] triazine-2-yl] benzonitrile, we must carefully examine the current market conditions, consult the industry, or visit the market, business network, to obtain a more accurate number. Unfortunately, I do not know the current market conditions, so it is difficult to understand the scope of its valuation. However, if you want to know its price, you can follow the above method and investigate it in detail, and you can get the actual price range.